Canonical Allele Identifier: CA360400990
Community Standard Title: NM_032119.4(ADGRV1):c.9717G>A (p.Trp3239Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90721028G>A , CM000667.2:g.90721028G>A GRCh38
NC_000005.9:g.90016845G>A , CM000667.1:g.90016845G>A GRCh37
NC_000005.8:g.90052601G>A NCBI36
NG_007083.1:g.167229G>A
NG_007083.2:g.196685G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.9717G>A MANE Select NP_115495.3:p.Trp3239Ter
ENST00000405460.9:c.9717G>A MANE Select ENSP00000384582.2:p.Trp3239Ter
NM_032119.3:c.9717G>A NP_115495.3:p.Trp3239Ter
NR_003149.1:n.9730G>A
NR_003149.2:n.9733G>A
ENST00000405460.6:c.9717G>A ENSP00000384582.2:p.Trp3239Ter
ENST00000509621.1:c.2414G>A
ENST00000639431.1:c.265+44819G>A ENSP00000491057.1:n.265+44819G>A
ENST00000640374.1:n.2861G>A
ENST00000640464.1:n.136G>A
ENST00000640779.1:c.4446G>A
XM_011543675.1:c.9714G>A XP_011541977.1:p.Trp3238Ter
XM_011543676.1:c.9636G>A XP_011541978.1:p.Trp3212Ter
XM_011543677.1:c.7020G>A XP_011541979.1:p.Trp2340Ter
XM_011543678.1:c.9717G>A XP_011541980.1:p.Trp3239Ter
XM_011543679.1:c.9717G>A XP_011541981.1:p.Trp3239Ter
XM_017009963.2:c.9738G>A XP_016865452.1:p.Trp3246Ter
XM_017009964.2:c.9735G>A XP_016865453.1:p.Trp3245Ter
XM_017009965.1:c.9735G>A XP_016865454.1:p.Trp3245Ter
XM_017009966.2:c.9657G>A XP_016865455.1:p.Trp3219Ter
XM_017009967.1:c.9642G>A XP_016865456.1:p.Trp3214Ter
XM_017009968.2:c.9738G>A XP_016865457.1:p.Trp3246Ter
XM_017009969.2:c.9738G>A XP_016865458.1:p.Trp3246Ter
XM_017009970.2:c.9738G>A XP_016865459.1:p.Trp3246Ter
XM_017009971.2:c.9738G>A XP_016865460.1:p.Trp3246Ter
XM_017009972.1:c.2856G>A XP_016865461.1:p.Trp952Ter
XM_017009973.1:c.2835G>A XP_016865462.1:p.Trp945Ter
XM_017009974.2:c.9738G>A XP_016865463.1:p.Trp3246Ter
XR_001742802.1:n.2523-5219C>T
XR_948560.1:n.272-5219C>T